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Investigative Ophthalmology & Visual Science
|
April 4, 2024
ERG Responses in Albinism, Idiopathic Infantile Nystagmus, and Controls
Zhanhan Tu, Christopher Degg, Michael Bach, et al.
Bioresource Technology
|
June 27, 2017
Effect of salt type and concentration on the growth and lipid content of Chlorella vulgaris in synthetic saline wastewater for biofuel production
Jared Church, Jae-Hoon Hwang, Keug-Tae Kim, et al.
Australian Journal of Psychology
|
July 16, 2025
Use of measures and measurement-based care in child and youth mental health: a survey of Australian practitioners
Lucy A Tully, Janice Kan, Adrienne Turnell, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
August 29, 2023
Learning With a Supervisor Who has Traffic Offences and Young Driver Crashes: The DRIVE Study 13-Year Follow-Up
Teresa Senserrick, Holger Möller, Soufiane Boufous, et al.
Injury Prevention : Journal of the International Society for Child and Adolescent Injury Prevention
|
February 22, 2023
Self-harm in adolescence and risk of crash: a 13-year cohort study of novice drivers in New South Wales, Australia
Patricia Cullen, Holger Mőller, Rachel Baffsky, et al.
Injury Prevention : Journal of the International Society for Child and Adolescent Injury Prevention
|
September 28, 2022
Acculturation and risk of traffic crashes in young Asian-born Australian drivers
Soufiane Boufous, Holger Möller, George Patton, et al.
Human Molecular Genetics
|
August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
Helen J Kuht, Jinu Han, Gail D E Maconachie, et al.
Applied and Environmental Microbiology
|
March 13, 2021
Prevalence and Epidemiology of Non-O157 Escherichia coli Serogroups O26, O103, O111, and O145 and Shiga Toxin Gene Carriage in Scottish Cattle, 2014-2015
Deborah V Hoyle, Marianne Keith, Helen Williamson, et al.
Brain : a Journal of Neurology
|
March 29, 2008
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7
Shery Thomas, Frank A Proudlock, Nagini Sarvananthan, et al.
Human Mutation
|
March 3, 2019
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
Christina Zeitz, Christelle Michiels, Marion Neuillé, et al.
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Showing results (11-20 of 20) with videos related to
Sort By:
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You have reached the last page of results.
This site can display upto 20 results.
Investigative Ophthalmology & Visual Science
|
April 4, 2024
ERG Responses in Albinism, Idiopathic Infantile Nystagmus, and Controls
Zhanhan Tu, Christopher Degg, Michael Bach, et al.
Bioresource Technology
|
June 27, 2017
Effect of salt type and concentration on the growth and lipid content of Chlorella vulgaris in synthetic saline wastewater for biofuel production
Jared Church, Jae-Hoon Hwang, Keug-Tae Kim, et al.
Australian Journal of Psychology
|
July 16, 2025
Use of measures and measurement-based care in child and youth mental health: a survey of Australian practitioners
Lucy A Tully, Janice Kan, Adrienne Turnell, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
August 29, 2023
Learning With a Supervisor Who has Traffic Offences and Young Driver Crashes: The DRIVE Study 13-Year Follow-Up
Teresa Senserrick, Holger Möller, Soufiane Boufous, et al.
Injury Prevention : Journal of the International Society for Child and Adolescent Injury Prevention
|
February 22, 2023
Self-harm in adolescence and risk of crash: a 13-year cohort study of novice drivers in New South Wales, Australia
Patricia Cullen, Holger Mőller, Rachel Baffsky, et al.
Injury Prevention : Journal of the International Society for Child and Adolescent Injury Prevention
|
September 28, 2022
Acculturation and risk of traffic crashes in young Asian-born Australian drivers
Soufiane Boufous, Holger Möller, George Patton, et al.
Human Molecular Genetics
|
August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
Helen J Kuht, Jinu Han, Gail D E Maconachie, et al.
Applied and Environmental Microbiology
|
March 13, 2021
Prevalence and Epidemiology of Non-O157 Escherichia coli Serogroups O26, O103, O111, and O145 and Shiga Toxin Gene Carriage in Scottish Cattle, 2014-2015
Deborah V Hoyle, Marianne Keith, Helen Williamson, et al.
Brain : a Journal of Neurology
|
March 29, 2008
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7
Shery Thomas, Frank A Proudlock, Nagini Sarvananthan, et al.
Human Mutation
|
March 3, 2019
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
Christina Zeitz, Christelle Michiels, Marion Neuillé, et al.
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of 2